The Pre-treatment Lymphocyte-to-Monocyte Ratio Predicts Efficacy in Metastatic Colorectal Cancer Treated With TAS-102 and Bevacizumab

被引:15
|
作者
Kuramochi, Hidekazu [1 ]
Yamada, Takeshi [2 ]
Yoshida, Yoichiro [3 ]
Matsuda, Akihisa [2 ]
Kamiyama, Hirohiko [4 ]
Kosugi, Chihiro [5 ]
Ishibashi, Keiichiro [6 ]
Fukazawa, Atsuko [7 ]
Ihara, Keisuke [8 ]
Sonoda, Hiromichi [2 ]
Yoshimatsu, Kazuhiko [9 ]
Yoshida, Hiroshi [2 ]
Hasegawa, Suguru [3 ]
Sakamoto, Kazuhiro [4 ]
Ishida, Hideyuki [6 ]
Koda, Keiji [5 ]
机构
[1] Tokyo Womens Med Univ, Yachiyo Med Ctr, Dept Chemotherapy, Yachiyo, Japan
[2] Nippon Med Sch, Dept Gastrointestinal & Hepatobiliary Pancreat Su, Tokyo, Japan
[3] Fukuoka Univ, Dept Gastroenterol Surg, Fac Med, Fukuoka, Japan
[4] Juntendo Univ, Dept Coloproctol Surg, Fac Med, Tokyo, Japan
[5] Teikyo Univ, Dept Surg, Chiba Med Ctr, Ichihara, Chiba, Japan
[6] Saitama Med Univ, Saitama Med Ctr, Dept Digest Tract & Gen Surg, Kawagoe, Saitama, Japan
[7] Iwata City Hosp, Dept Gastroenterol Surg, Iwata, Japan
[8] Dokkyo Med Univ, Dept Surg 1, Mibu, Tochigi, Japan
[9] Kawasaki Med Sch, Dept Digest Surg, Kurashiki, Okayama, Japan
关键词
TAS-102; bevacizumab; colorectal cancer; lymphocyteto-monocyte ratio (LMR); neutrophil-to-lymphocyte ratio (NLR); PROGNOSTIC-SIGNIFICANCE; OPEN-LABEL; SURVIVAL; INFLAMMATION;
D O I
10.21873/anticanres.15098
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Our multicenter phase II TAS-CC3 study demonstrated favorable median progression-free survival (PFS) and overall survival (OS) of 32 metastatic colorectal cancer (mCRC) patients treated with TAS-102 + bevacizumab as 3rd-line treatment. Patients and Methods: We investigated the predictive and prognostic values of pretreatment blood inflammation-based scores, including the neutrophil-to-lymphocyte (NLR), platelet-to-lymphocyte (PLR) and lymphocyte-to-monocyte ratio (LMR) on disease-control (DC), PFS and OS by a post-hoc analysis. Results: Receiver operating characteristic curve analyses of the 3 inflammation-based scores versus DC showed the best predictive performance for LMR, followed by NLR and PLR. The high-LMR group had a significantly higher DC rate than the low group (87.5 vs. 43.8%). The high-LMR group showed significantly longer survival than the low group (4.9 vs. 23 m for median PFS) (21.0 vs. 6.1 m for median OS). Conclusion: The pre-treatment LMR is a valid predictive and prognostic biomarker for mCRC patients undergoing TAS-102 and bevacizumab treatment.
引用
收藏
页码:3131 / 3137
页数:7
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